Evidence mapPaperPMID 41867376Full record

ArticleMolecular vision2025

Prevention of diabetic retinopathy in a rat model by a functional food mix.

Krishna Kalyan Kalahasti, Pandarinath Savitikadi, Ch Uday Kumar, Marka Nagaraju, S Sreenivasa Reddy, G Bhanuprakash Reddy

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Article in Molecular vision, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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6 authors.

Krishna Kalyan KalahastiBiochemistry Division, ICMR-National Institute of Nutrition, Hyderabad, 500007, India.
Pandarinath SavitikadiBiochemistry Division, ICMR-National Institute of Nutrition, Hyderabad, 500007, India.
Ch Uday KumarBiochemistry Division, ICMR-National Institute of Nutrition, Hyderabad, 500007, India.
Marka NagarajuBiochemistry Division, ICMR-National Institute of Nutrition, Hyderabad, 500007, India.
S Sreenivasa ReddyBiochemistry Division, ICMR-National Institute of Nutrition, Hyderabad, 500007, India.
G Bhanuprakash ReddyBiochemistry Division, ICMR-National Institute of Nutrition, Hyderabad, 500007, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Diabetic retinopathy (DR), a severe microvascular complication of both type 1 and type 2 diabetes, is one of the leading causes of blindness. Prolonged hyperglycemia leads to vascular endothelial changes, inflammation, neovascularization, and apoptosis through multiple mechanisms, including increased aldose reductase (AR) activity and formation of advanced glycation end products, which contribute to the development of DR. Based on our previous studies with various functional foods that showed AR inhibition and prevented the formation of advanced glycation end products, in this study, a functional food (FF) mix was formulated and investigated its efficacy against DR progression in a rat model. Methods: An FF mix was prepared with powders of amla pericarp, turmeric rhizome, ginger rhizome, cinnamon bark, and black pepper seeds in a specific proportion. Two-month-old Sprague-Dawley rats were grouped into control (C), streptozotocin-induced diabetes (D), and diabetes fed with FF at two levels (FF1, 0.85 g/100 g diet; FF2, 4.25 g/100 g diet) for 6 months from the induction of diabetes. At the end of the experiment, electroretinography was performed, and the eyes were dissected after the animals were sacrificed. A set of eyes was formalin-fixed for histology and immunohistochemistry examination, and the retina from the remaining eyes was used for immunoblotting analysis. Results: Supplementation of FF mix in the diet to diabetic rats has improved retinal function (electroretinography), as well as prevented histomorphological changes and loss of photoreceptor cells (rhodopsin), compared to untreated diabetic rats. Further, FF mix ameliorated hyperglycemia-induced angiogenesis (vascular endothelial growth factor, hypoxia-inducible factor 1α) and gliosis (glial fibrillary acidic protein) in the diabetic rats, accompanied by decreased inflammation (phosphorylated nuclear factor κB, tumor necrosis factor α, monocyte chemoattractant protein 1) and apoptosis (Bax, Bcl2, caspase3, and caspase12). Conclusions: This study illustrates the potential of an FF mix, attributed to the synergistic effects of its components, alleviating the progression of diabetic retinopathy by reducing diabetes-induced hypoxia, gliosis, and inflammation, while also inhibiting apoptosis in retinal cells.

Indexed as

Diabetes Mellitus, ExperimentalDiabetic RetinopathyAldehyde ReductaseAnimalsApoptosisbcl-2-Associated X ProteinBlood GlucoseDisease Models, AnimalElectroretinographyMaleRatsRats, Sprague-DawleyRetinaVascular Endothelial Growth Factor AAldehyde Reductasebcl-2-Associated X ProteinBlood GlucoseVascular Endothelial Growth Factor A

Identifiers

PMID41867376
PMCPMC13002552

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.